High-power radiofrequency ablation for ventricular tachycardia in patients with structural heart disease: one-year follow-up data from the multicenter prospective registry

Q4 Medicine
S. Korolev, E. Artyukhina, V. Shabanov, O. Sapelnikov, A. Tsyganov, A. Revishvili, A. Romanov
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引用次数: 1

Abstract

Background: The outcomes of ventricular tachycardia (VT) ablation in patients with structural heart disease (SHD) are not ideal. High-power radiofrequency ablation (RFA) may have a long-term beneficial effect in this patient cohort.Objective: To evaluate the safety, early and long-term efficacy of high-power RFA for VT and concomitant SHD in a multicenter prospective registry.Methods: Our study included a total of 63 patients (66,7% of them were men; median age was 61.0 [51.0-66.5] years) with ischemic heart disease and drug-resistant VT who were scheduled for RFA (50 W). Non-fluoroscopic 3D mapping systems were used for bipolar and activation mapping with standard settings. The safety end point included perioperative complications, such as death, hemopericardium, stroke, myocardial infarction, electrical storm, and vascular complications. The efficacy end points included VT non-inducibility at the end of ablation and freedom from VT at 12 months of the follow-up. The secondary end points were changes in implantable cardioverter-defibrillator (ICD) therapy, sonographic findings, and number of hospital admissions.Results: All patients underwent VT ablation under general sedation. One clinical VT was induced in 96.8% of the patients before ablation. After ablation no clinical VTs were induced (P < .0001 vs baseline). No perioperative complications were observed. Freedom from VT without antiarrhythmic drugs was 82.6% at 12 months of the follow-up. The number of ICD therapies significantly decreased at 12 months of the follow-up compared with baseline (3.2% vs 31.7%, respectively; P = .0001). The left ventricular ejection fraction increased from 48.7% ± 14.7% at baseline to 50.3% ± 11.9% at 12 months of the follow-up (P = .038). There was a statistically significant decrease in hospital admission rate before and after ablation (from 2 [range: 0-12] to 0 [range: 0-3], P < .0001).Conclusion: High-power RFA for VT in patients with ischemia demonstrated its safety and high perioperative and long-term efficacy, which were linked to clinical improvement. Further randomized studies will help introduce this VT ablation approach into routine clinical practice. Received 5 September 2022. Revised 16 February 2023. Accepted 31 May 2023. Funding: The study did not have sponsorship. Conflict of interest: The authors declare no conflict of interest. Contribution of the authorsConception and study design: S.V. Korolev, A.Sh. Revishvili, A.B. Romanov Data collection and analysis: S.V. Korolev, E.A. Artyukhina, V.V. Shabanov, O.V. Sapelnikov, A.V. Tsyganov, A.Sh. Revishvili, A.B. RomanovStatistical analysis: S.V. Korolev Drafting the article: S.V. Korolev Critical revision of the article: A.B. Romanov, A.Sh. Revishvili Final approval of the version to be published: S.V. Korolev, E.A. Artyukhina, V.V. Shabanov, O.V. Sapelnikov, A.V. Tsyganov, A.Sh. Revishvili, A.B. Romanov
高功率射频消融治疗结构性心脏病患者室性心动过速:来自多中心前瞻性登记的一年随访数据
背景:室性心动过速(VT)消融术治疗结构性心脏病(SHD)的效果并不理想。高功率射频消融术(RFA)在该患者队列中可能具有长期有益的效果。目的:在一项多中心前瞻性研究中,评价高功率射频消融治疗VT及合并SHD的安全性、早期和长期疗效。方法:本研究共纳入63例患者(66.7%为男性;中位年龄为61.0[51.0-66.5]岁,伴有缺血性心脏病和耐药室速,计划进行RFA (50 W)。非透视3D制图系统用于双极和标准设置的激活制图。安全性终点包括围手术期并发症,如死亡、心包积血、中风、心肌梗死、电风暴和血管并发症。疗效终点包括消融结束时室速无诱导性和随访12个月时无室速。次要终点是植入式心律转复除颤器(ICD)治疗的变化、超声检查结果和住院人数。结果:所有患者均在全身镇静下行房室消融术。96.8%的患者在消融前发生1次临床室速。消融后无临床室性心动过速(P < 0.05)。0001 vs基线)。无围手术期并发症。随访12个月时,无抗心律失常药物的室性心动过速自由率为82.6%。随访12个月时,与基线相比,ICD治疗的次数显著减少(分别为3.2%对31.7%;p = 0.0001)。左室射血分数从基线时的48.7%±14.7%上升至随访12个月时的50.3%±11.9% (P = 0.038)。消融前后住院率下降有统计学意义(从2[范围:0-12]降至0[范围:0-3],P < 0.0001)。结论:大功率射频消融术治疗VT缺血患者安全性高,围手术期和远期疗效高,与临床改善有关。进一步的随机研究将有助于将VT消融方法引入常规临床实践。2022年9月5日收到。2023年2月16日修订。2023年5月31日录用。经费来源:本研究未获得赞助。利益冲突:作者声明无利益冲突。作者贡献。研究构思与设计:S.V. Korolev, A.Sh。数据收集与分析:S.V. Korolev, E.A. Artyukhina, V.V. Shabanov, O.V. Sapelnikov, A.V. Tsyganov, A.Sh。统计分析:S.V.科罗廖夫文章起草:S.V.科罗廖夫文章评论修订:A.B.罗曼诺夫,a.h.。最终批准出版的版本:S.V.科罗廖夫,E.A.阿图奇娜,V.V.沙巴诺夫,O.V.萨佩尔尼科夫,A.V.茨加诺夫,a.s.。莱什维利,A.B.罗曼诺夫
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来源期刊
Patologiya krovoobrashcheniya i kardiokhirurgiya
Patologiya krovoobrashcheniya i kardiokhirurgiya Medicine-Cardiology and Cardiovascular Medicine
CiteScore
1.00
自引率
0.00%
发文量
42
审稿时长
12 weeks
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